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NCT05828394

Palate Wound Healing and Pain Perception of De-epthelized Ctg vs Sub-epithelial Ctg

Completed NA Last updated 8 May 2024
What this trial tests

NA trial testing DFGG in Palate; Wound in 32 participants. Completed in 7 May 2024.

Timeline
15 February 2023
Primary endpoint
7 May 2024
7 May 2024

Quick facts

Lead sponsorUniversitat Internacional de Catalunya
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment32
Start date15 February 2023
Primary completion7 May 2024
Estimated completion7 May 2024
Sites2 locations across Spain

Drugs / interventions tested

Conditions studied

Sponsor

Universitat Internacional de Catalunya — full company profile →

Who can join

Adults 18 to 70, any sex, with Palate; Wound. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

A single blinded randomized clinical trial was designed to evaluate the influence of palatal harvesting technique on post-operatory patient pain perception. The participants will be selected between subjects in need of at least one mucogingival procedure involving the harvesting of a connective tissue graft and then randomly allocated in the following groups. Two harvesting techniques were chosen to be compared: de-epithelialized free gingival graft (DFGG) and subepithelial connective tissue graft (SCTG).

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Palate; Wound

Currently open trials in the same condition.

Other Universitat Internacional de Catalunya trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05828394.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing